rs11014002
A SNP in the KIAA1217 gene on chromosome 10. Its most notable genotype is C;C: common in complete genomics
- Gene
- KIAA1217
- Location
- Chr 1024,275,724 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 9%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 8 HapMap populations.
- AverageC;C 86%
- European ancestry (Utah)C;C 86%
- Han Chinese (Beijing)C;C 58%
- Japanese (Tokyo)C;C 68%
- Yoruba (Nigeria)C;C 100%
- African ancestry (Southwest US)C;C 95%
- Luhya (Kenya)C;C 98%
- Mexican ancestry (Los Angeles)C;C 91%
- TuscanC;C 88%
Related
Notes
From SNPedia
Notes
Association of the tag SNPs in the human SKT gene (KIAA1217) with lumbar disc herniation. Comprehensive analysis of the impact of SNPs and CNVs on human microRNAs and their regulatory genes.
Source and license
Adapted from rs11014002 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.